Journal article
HbA1c and mean glucose derived from short-term continuous glucose monitoring assessment do not correlate in patients with HbA1c >8
- Abstract:
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Aims
Optimum therapy for patients with diabetes depends on both acute and long-term changes in plasma glucose, generally assessed by HbA1c levels. However, the correlation between HbA1c and circulating glucose has not been fully determined. Therefore, we carefully examined this correlation when glucose levels were assessed by continuous glucose monitoring (CGM).
Methods
51 patients (70 % women, 30% male) were examined; among them were 28 type 1 patients with diabetes and 23 type 2 patients with diabetes. Clinically determined HbA1c levels were compared with blood glucose determined by CGM during a short time period. Results: Changes of HbA1c levels up to 8.0% showed a clear and statistically strong correlation (R=0.6713, P<0.0001) with mean blood glucose levels measured by CGM, similarly to that observed in the A1c-derived Average Glucose (ADAG) study where patients were monitored for a longer period. However, we found no statistical correlation (R=0.0498, P=0.8298) between HbA1c and CGM-assessed glucose levels in our patient population when HbA1c was greater than 8.0 %
Results
Changes of HbA1c levels up to 8.0% showed a clear and statistically strong correlation (R=0.6713, P<0.0001) with mean blood glucose levels measured by CGM, similarly to that observed in the A1c-derived Average Glucose (ADAG) study where patients were monitored for a longer period. However, we found no statistical correlation (R=0.0498, P=0.8298) between HbA1c and CGM-assessed glucose levels in our patient population when HbA1c was greater than 8.0 %
Conclusions
Short term CGM appears to be a good clinical indicator of long-term glucose control (HbA1c levels), however cautions should be taken while interpreting CGM data from patients with HbA1c levels above 8.0%. Over or under estimation of the actual mean glucose from CGM data could potentially increase the risks of inappropriate treatment. As such, our results indicate that a more accurate analysis of CGM data might be useful to adequately tailor clinical treatments.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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- Files:
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(Preview, Accepted manuscript, pdf, 493.1KB, Terms of use)
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- Publisher copy:
- 10.4158/ep161363.or
Authors
- Publisher:
- American Association of Clinical Endocrinologists
- Journal:
- Endocrine Practice More from this journal
- Volume:
- 23
- Issue:
- 1
- Pages:
- 10-16
- Publication date:
- 2016-09-01
- Acceptance date:
- 2016-08-28
- DOI:
- EISSN:
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1934-2403
- ISSN:
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1530-891X
- Pmid:
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27631849
- Language:
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English
- Keywords:
- Pubs id:
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pubs:646059
- UUID:
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uuid:0cf8e651-4233-4a93-abe2-d00aa914f866
- Local pid:
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pubs:646059
- Source identifiers:
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646059
- Deposit date:
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2018-03-21
Terms of use
- Copyright holder:
- American Association of Clinical Endocrinologists
- Copyright date:
- 2016
- Notes:
- © 2016 AACE. This is the accepted manuscript version of the article. The final version is available online from American Association of Clinical Endocrinologists at: http://dx.doi.org/10.4158/ep161363.or
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